Required / Expected Competencies:

Registered doctor with MBChB and 2+ years clinical research experience.
Current HPCSA registration and medical malpractice insurance.
Strong knowledge and skills in general medical practice.
Effective decision-making and collaboration skills.
Thorough knowledge of ICH GCP.
Meticulous attention to detail in patient data recording.
Completion and management of study documentation.
Professional attitude and proactive communication with colleagues.
Commitment to professional development.
Proficiency in MS Word, Excel, PowerPoint.
Advantageous: previous clinical research experience, proficiency in Tswana and/or Zulu.

Core Functions will include but not limited to:

Direct and oversee research activities, ensuring research integrity and compliance.
Manage research projects administratively.
Conduct unbiased research in line with regulations.
Ensure accurate, ethical, and efficient clinical trial processes.
Conduct clinical trials and provide medical oversight.
Liaise with stakeholders and clients.
Ensure adherence to ICH GCP and local guidelines.
Apply clinical knowledge per protocol.
Participate in and initiate trial data publications.
Oversee regulatory processes, participant recruitment, quality assurance, and laboratory/pharmacy tasks.
Facilitate participant recruitment and informed consent.
Manage participants clinically as per protocols.
Conduct and attend relevant training.
Review and action laboratory results.
Interpret ECGs, CXRs, etc.
Address monitoring and data queries.
Review and draft SOPs.
Prepare source documents.
Report adverse events.
Engage in community education and clinic patient care.
Train and develop staff and students in clinical research.